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What resources are you aware of that could help people with sickle cell? Websites? Organizations? Books? Programs?

  1. These are the books that I believe are good to start with.1.Simone C. Eastman Uwan M.D.
    'A Doctor In A Patient's Body: Dreaming Big With Sickle Cell Disease And Chronic Pain'

    2. 'Adversity Introduced Me to Me: A Memoir' By
    3. 'Mixed Blessings from a Cambridge Union' By

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